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用于不同小反刍兽疫病毒株和牛瘟病毒株的微量中和系统。

Microneutralisation systems for use with different strains of peste des petits ruminants virus and rinderpest virus.

作者信息

Rossiter P B, Jessett D M, Taylor W P

出版信息

Trop Anim Health Prod. 1985 May;17(2):75-81. doi: 10.1007/BF02360775.

Abstract

Comparative studies were made to determine the most suitable microtitration system for assaying strains of peste des petits ruminants virus (PPRV) and rinderpest virus (RV). Infectivity titres did not differ significantly when assayed in either calf kidney, sheep kidney or Vero cells. However, cytopathic effects were much easier to detect in the latter making them the cell of choice. Addition of small amounts of virus to preformed cell monolayers in microplates with the subsequent addition of maintenance medium give higher infectivity titres than when cell suspension was added to virus, although the latter is more convenient for routine use. The titres of PPRV and neutralising antibodies assayed in tubes and microplates were not significantly different. Simultaneous screening of sera at a 1 in 20 dilution against both PPRV and RV gave a higher incidence of positives against homologous as opposed to heterologous virus.

摘要

进行了比较研究,以确定用于检测小反刍兽疫病毒(PPRV)和牛瘟病毒(RV)毒株的最合适微量滴定系统。在犊牛肾、绵羊肾或Vero细胞中进行检测时,感染性滴度没有显著差异。然而,在后一种细胞中更容易检测到细胞病变效应,这使其成为首选细胞。向微孔板中预先形成的细胞单层中加入少量病毒,随后加入维持培养基,比将细胞悬液加入病毒中能获得更高的感染性滴度,尽管后者在常规使用中更方便。在试管和微孔板中检测的PPRV中和抗体滴度没有显著差异。以1:20稀释度同时对PPRV和RV进行血清筛查时,针对同源病毒而非异源病毒的阳性发生率更高。

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